A self‐powered system to electrochemically generate ammonia driven by palladium single atom electrocatalyst
Hao Hu,
Shuyuan Pan,
Zhiyong Ma,
Kaiyi Liu,
Yi Li,
Haifeng Bao,
Chengwei Deng,
Fang Luo,
Zehui Yang
Affiliations
Hao Hu
State Key Laboratory of New Textile Materials & Advanced Processing Technology College of Materials Science and Engineering Wuhan Textile University Wuhan China
Shuyuan Pan
Faculty of Materials Science and Chemistry China University of Geosciences Wuhan China
Zhiyong Ma
Shaanxi Coal Chemical Industry Technology Research Institute Co., Ltd. Xi'an China
Kaiyi Liu
Shaanxi Coal Chemical Industry Technology Research Institute Co., Ltd. Xi'an China
Yi Li
Shaanxi Coal Chemical Industry Technology Research Institute Co., Ltd. Xi'an China
Haifeng Bao
State Key Laboratory of New Textile Materials & Advanced Processing Technology College of Materials Science and Engineering Wuhan Textile University Wuhan China
Chengwei Deng
State Key Laboratory of Space Power‐Sources Technology Shanghai Institute of Space Power Sources Shanghai China
Fang Luo
State Key Laboratory of New Textile Materials & Advanced Processing Technology College of Materials Science and Engineering Wuhan Textile University Wuhan China
Zehui Yang
Faculty of Materials Science and Chemistry China University of Geosciences Wuhan China
Abstract The utilization of single atoms (SAs) as trifunctional electrocatalyst for nitrogen reduction, oxygen reduction, and oxygen evolution reactions (NRR, ORR, and OER) is still a formidable challenge. Herein, we devise one‐pot synthesized palladium SAs stabilized on nitrogen‐doped carbon palladium SA electrocatalyst (Pd‐SA/NC) as efficient trifunctional electrocatalyst for NRR, ORR, and OER. Pd‐SA/NC performs a robust catalytic activity toward NRR with faradaic efficiency of 22.5% at −0.25 V versus reversible hydrogen electrode (RHE), and the relative Pd utilization efficiency is enhanced by 17‐fold than Pd‐NP/NC. In addition, the half‐wave potential reaches 0.876 V versus RHE, amounting to a 58‐time higher mass activity than commercial Pt/C. Moreover, the overpotential at 10 mA cm−2 is as low as 287 mV for Pd‐SA/NC, outperforming the commercial IrO2 by 360 times in turnover frequency at 1.6 V versus RHE. Accordingly, the assembled rechargeable zinc‐air battery (ZAB) achieves a maximum power density of 170 mW cm−2, boosted by 2.3 times than Pt/C–IrO2. Two constructed ZABs efficiently power the NRR‐OER system to electrochemically generate ammonia implying its superior trifunctionality.